Canonical Allele Identifier: PA2741810999
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831060
ClinVar RCV Id: RCV003678963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Arg1393Pro
CA403615578
NM_000064.4:c.4178G>C